Can a simple floss band beat metal tools for Post-Surgery knee pain?
NCT ID NCT07204119
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests two non-drug treatments—Graston Technique (using metal tools) and Tissue Flossing (using elastic bands)—to see which works better for knee stiffness after fracture surgery. 48 adults aged 20-40 with limited knee motion will be randomly assigned to one of the two therapies or a control group. Researchers will measure pain, range of motion, and daily function over six months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Graston Technique and Tissue Flossing Technique
- What this could lead to
- If one technique works better, it could offer a simple, drug-free way to improve knee movement and reduce pain after surgery.
- What could go wrong
- This is a small, early-stage trial with only 48 people, so results may not apply to everyone. The techniques are manual therapies, and benefits may be modest or temporary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 48 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Dec 2025
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 40 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age group between 20 to 40 years. 2. Both male and female. 3. Patients with 6 weeks post-operative following open reduction and internal fixation (ORIF) of femur, tibia, or fibula shaft fracture 4. Decreased in knee Flexion \& Extension (A minimum of 20° or above). Exclusion criteria: 1. Those patients who have allergies to latex 2. Malignant or metabolic cause of knee fracture 3. Venous Thrombotic disease/ Varicose veins. 4. Cardiopulmonary illness and hypertension. 5. Skin diseases/ metabolic disorders. 6. Patient with arthroplasty and arthroscopy. 7. Patellar fracture/ ACL/ PCL/ MCL/ LCL rupture/ injuries. 8. Any pathological condition having effects on knees.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Banazir Bhutto Hospital,
RECRUITINGRawalpindi, Punjab Province, 46000, Pakistan